Frontal polymerization in multifunctional thiol-ene systems was demonstrated. For an ene that could not undergo free-radical-chain propagation, the front velocity and front temperature were a maximum at the stoichiometric ratio of the thiol and ene. For a system like HDDA, which can homopolymerize as well as copolymerize with the thiol, the addition of even a small amount of thiol increased the front velocity by as much as 80% by reducing oxygen inhibition.
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Pojman et al. (2004) studied this question.
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